A neuropeptide antagonist
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Antagonist G (trifluoroacetate salt)

Item No. 34425

Technical Information
Formal Name
L-arginyl-D-tryptophyl-N-methyl-L-phenylalanyl-D-tryptophyl-L-leucyl-L-methioninamide, trifluoroacetate salt
Synonyms
  • Arg-D-Trp-NmePhe-D-Trp-Leu-Met-NH2
  • [Arg6,D-Trp7,9,NmePhe8]-Substance P (6-11)
  • [Arg6,D-Trp7,9,NmePhe8]-SP (6-11)
Molecular Formula
C49H66N12O6S • XCF3COOH
Formula Weight
Purity
≥98%
A solid
DMF: 30 mg/mlDMSO: 30 mg/mlDMSO:PBS (pH 7.2) (1:3): 0.25 mg/mlEthanol: 20 mg/ml
λmax
220 nm
SMILES
CSCC[C@@H](C(N)=O)NC([C@H](CC(C)C)NC([C@@H](CC1=CNC2=CC=CC=C12)NC([C@H](CC3=CC=CC=C3)N(C)C([C@H](NC([C@@H](N)CCCNC(N)=N)=O)CC4=CNC5=CC=CC=C45)=O)=O)=O)=O.OC(C(F)(F)F)=O
InChi Code
InChI=1S/C49H66N12O6S.C2HF3O2/c1-29(2)23-39(45(64)57-38(43(51)62)20-22-68-4)58-46(65)40(25-31-27-55-36-18-10-8-15-33(31)36)59-47(66)42(24-30-13-6-5-7-14-30)61(3)48(67)41(26-32-28-56-37-19-11-9-16-34(32)37)60-44(63)35(50)17-12-21-54-49(52)53;3-2(4,5)1(6)7/h5-11,13-16,18-19,27-29,35,38-42,55-56H,12,17,20-26,50H2,1-4H3,(H2,51,62)(H,57,64)(H,58,65)(H,59,66)(H,60,63)(H4,52,53,54);(H,6,7)/t35-,38-,39-,40+,41+,42-;/m0./s1
InChi Key
GUDATFWCKFMCTO-RGVCNNQFSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Antagonist G is a neuropeptide antagonist.1,2,3 It inhibits the binding of vasopressin to rat liver or Swiss 3T3 membranes (IC50s = 3.5 and 2.2 µM, respectively) and vasopressin-induced production of inositol phosphate in Swiss 3T3 fibroblasts (IC50 = 1 µM).1 Antagonist G (50 µM) induces apoptosis and the production of reactive oxygen species (ROS) in NCI H69 small cell lung cancer (SCLC) cells.2 It reduces tumor growth in an NCI H69 mouse xenograft model when administered at a dose of 45 µg/g.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Seckl, M.J., Newman, R.H., Freemont, P.S., et alSubstance P-related antagonists inhibit vasopressin and bombesin but not 5'-3-O-(thio)triphosphate-stimulated inositol phosphate production in swiss 3T3 cells. J. Cell Physiol. 163(1), 87-95 (1995).

    2. MacKinnon, A.C., Waters, C., Rahman, I., et al[Arg6, D-Trp7,9, NmePhe8]-substance P (6-11) (antagonist G) induces AP-1 transcription and sensitizes cells to chemotherapy. Br. J. Cancer. 83(7), 941-948 (2000).

    3. Langdon, S., Sethi, T., Ritchie, A., et alBroad spectrum neuropeptide antagonists inhibit the growth of small cell lung cancer in vivo. Cancer Res. 52(16), 4554-4557 (1992).